Haematology
Service
University Medical Center Hamburg-Eppendorf
Hamburgo, AlemaniaPublications in collaboration with researchers from University Medical Center Hamburg-Eppendorf (25)
2024
2023
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Integrating biological HLA-DPB1 mismatch models to predict survival after unrelated hematopoietic cell transplantation
Haematologica
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Molnupiravir compared to nirmatrelvir/ritonavir for COVID-19 in high-risk patients with haematological malignancy in Europe. A matched-paired analysis from the EPICOVIDEHA registry
International Journal of Antimicrobial Agents, Vol. 62, Núm. 4
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Passive pre-exposure immunization by tixagevimab/cilgavimab in patients with hematological malignancy and COVID-19: matched-paired analysis in the EPICOVIDEHA registry
Journal of hematology & oncology
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von Willebrand factor neutralizing and non-neutralizing alloantibodies in 213 subjects with type 3 von Willebrand disease enrolled in 3WINTERS-IPS
Journal of Thrombosis and Haemostasis, Vol. 21, Núm. 4, pp. 787-799
2022
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Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study
Journal of Thrombosis and Haemostasis, Vol. 20, Núm. 5, pp. 1106-1114
2020
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Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS-IPS, an international and collaborative cross-sectional study
Journal of Thrombosis and Haemostasis, Vol. 18, Núm. 9, pp. 2145-2154
2019
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Pomalidomide, bortezomib, and dexamethasone for patients with relapsed or refractory multiple myeloma previously treated with lenalidomide (OPTIMISMM): a randomised, open-label, phase 3 trial
The Lancet Oncology, Vol. 20, Núm. 6, pp. 781-794
2015
2013
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VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease
Blood, Vol. 121, Núm. 12, pp. 2336-2339
2011
2010
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ITER study of patients with haemo philia A and factor VIII inhibitors
Hamostaseologie, Vol. 30, Núm. SUPPL.1, pp. 46-47
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Sequential combined bypassing therapy of bleeds unresponsive to a single bypassing agent Safety and efficacy: Safety and efficacy
Hamostaseologie, Vol. 30, Núm. SUPPL.1, pp. 54-55
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The impact of bleeding history, von willebrand factor and PFA-100® on the diagnosis of type 1 von willebrand disease: Results from the european study MCMDM-1VWD
British Journal of Haematology, Vol. 151, Núm. 3, pp. 245-251
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Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD
Thrombosis Research, Vol. 126, Núm. 3, pp. 227-231
2009
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Expression of 14 von Willebrand factor mutations identified in patients with type.1 von Willebrand disease from the MCMDM-1VWD study
Journal of Thrombosis and Haemostasis, Vol. 7, Núm. 8, pp. 1304-1312
2008
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Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)
Journal of Thrombosis and Haemostasis, Vol. 6, Núm. 5, pp. 762-771
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Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the european study: Molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD)
Blood, Vol. 111, Núm. 10, pp. 4979-4985
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Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): Results from the European Study MCMDM-1VWD
Blood, Vol. 111, Núm. 7, pp. 3531-3539
2007
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Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1VWD)
Journal of Thrombosis and Haemostasis, Vol. 5, Núm. 4, pp. 715-721